Table 2.
Study | Study Design | N | Treatment | Treatment Length | Instrument | Findings | |
---|---|---|---|---|---|---|---|
Sexual Function | Coital Incontinence | ||||||
Pelvic Floor Muscle Training (SUI) | |||||||
Bo et al [48] | Randomized controlled trial | 1. PMFT: 25 | PMFT | 6 months | B-FLUTS | • Non-significant improvement in pain, urinary-related sexual problems | • Improved |
2. Control: 30 | |||||||
Zahariou et al [49] | Prospective case series | Total: 58 | PFMT | 12 months | FSFI | • Improvement in FSFI and subscale scores (p < 0.05) | • Improved (p < 0.005) |
Pelvic Floor Muscle Training (UUI) | |||||||
Wang et al [50] | RCT | 1. PFMT: 34 | 1. PFMT | 12 weeks | KHQ: Personal Relationship Domain | • Non-significant improvement in Personal Relationship Domain in biofeedback-assisted PFMT group | N/A |
2. Biofeedback-assisted PFMT: 34 | 2. Biofeedback-assisted PFMT | ||||||
3. Transvaginal electrical stimulation: 35 | 3. Transvaginal electrical stimulation | ||||||
Anti-incontinence Pessary (SUI) | |||||||
Handa et al [52] | Randomized controlled trial | 1. Continence pessary: 149 | 1. Continence pessary | 12 months | SPEQ (3 domains), PISQ-12 | Responders (vs. non-responders): | • Improved (p = 0.0002) |
2. Behavioral therapy: 146 | 2. PMFT | • PISQ improved (p = 0.007) | • Greater improvement | ||||
3. Combo: 150 | 3. Combination | • Restriction of sex due to UI improved (p = 0.008) | • with combo therapy (p = 0.019) and behavioral (p = 0.02) vs. pessary alone | ||||
• Dyspareunia improved (p = 0.017) | |||||||
Transvaginal electrical stimulation (SUI and UUI) | |||||||
Giuseppe et al [51] | Prospective case series | Total: 23 | Transvaginal electrical stimulation | 3 months | FSFI | Significant improvement in FSFI and all subscale scores (p ≤ 0.01) except arousal, orgasm | N/A |
SUI: 8 | |||||||
UUI: 10 | |||||||
MUI: 5 | |||||||
Anti-cholinergic medication (UUI) | |||||||
Sand et al [53] | RCT | Total: 2878 | 1. Patient education & transdermal oxybutynin | 12 weeks | KHQ: Personal Relationship Domain | Significant improvement in KHQ score, bladder pain, effect of OAB on sex life, interest in sex | Improved |
Female: 2508 | 2. Transdermal oxybutynin only | ||||||
Rogers et al [54] | RCT | 1. Placebo: 189 | 1. Placebo | 12 weeks | PISQ | Significant improvement of PISQ and domain scores after 12 weeks | N/A |
2. Tolterodine: 188 | 2. Tolterodine 4 mg ER daily | Stable but no continued improvement if used 12 additional weeks except in Physical domain | |||||
Danilova et al [58] | Prospective case series | 57 | Trospium 15 mg three times daily | 16 weeks | Unknown | Sexual dysfunction decreased | N/A |
Chapple et al [56] | RCT | 1. Placebo: 283 | 1. Placebo | 12 weeks | KHQ: Personal Relationship Domain | Patients with OAB, total | N/A |
2. Fesoterodine 4/8 mg: 272 | 2. Fesoterodine 4 mg | Statistically significant improvement in fesoterodine 8 mg (vs. placebo) (mean score change of -11.9 v -6.2, p < 0.05) | |||||
3. Tolterodine ER 4 mg: 290 | 3. Fesoterodine 8 mg | Patients with both UUI & OAB: | |||||
4. Tolterodine ER 4 mg | Statistically significant improvement intolterodine (vs. placebo) (-12.7 v -6.8, p < 0.05) | ||||||
Percutaneous tibial nerve stimulation (UUI) | |||||||
Eftekhar et al [59] | RCT | 1. Percutaneous tibial nerve stimulation and tolterodine 4 mg daily: 25 | 1. Percutaneous tibial nerve stimulation and tolterodine 4 mg daily | 12 weeks | FSFI | Within each arm: | N/A |
2. Tolterodine 4 mg daily: 25 | 2. Tolterodine 4 mg daily | Significant improvement in FSFI and subscale scores after 12 weeks (p < 0.001) | |||||
Between arms: | |||||||
No significant difference in FSFI, subscale scores | |||||||
van Balken et al [60] | Prospective case series | Total: 121 | Percutaneous tibial nerve stimulation | 12 weeks | NSF-9 | Significant improvement in Satisfaction (p < 0.005), Frequency (p < 0.005), Orgasm (p < 0.05) | N/A |
Female: 76 | No significant change in dyspareunia, lubrication |
B-FLUTS Bristol female lower urinary tract symptoms; FSFI Female sexual function index; PISQ-12 Short form pelvic organ prolapse-urinary incontinence sexual function questionnaire; PFMT Pelvic floor muscle training; RCT Randomized controlled trial; SA Sexual activity; SPEQ: Short form personal experience questionnaire